A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1617n54



Internal ID22769512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5760659..5788000hg38UCSC Ensembl
chr11:5781889..5809230hg19UCSC Ensembl
chr11:5738465..5765806hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3827342
hg1927342
hg1827342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553313, nsv553314, nsv553316, nsv553315, nsv553312, nsv553318, nsv553317
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1617n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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